New program aims to cut risky meds in seniors
NCT ID NCT07671716
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study worked with patients and healthcare professionals to design a program that helps older adults safely stop taking medications that can cause confusion, falls, and other harms. The team held focus groups and workshops to understand barriers and create a step-by-step plan. The goal is to reduce hospital visits and improve quality of life for seniors on multiple medications.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could lead to a practical program that helps older adults safely stop taking risky medications, reducing falls and hospital visits.
- What could go wrong
- This is a small, completed study that only designed the program, not tested it. The actual benefits are unknown until tested in larger trials.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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35 people
The number who actually took part.
- Started
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Apr 2025
- Finished
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Jan 2026
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
* Hospital healthcare professionals involved in geriatric outpatient care and in the medication management of older patients: geriatricians, hospital pharmacists, and nurses * Primary care healthcare professionals involved in the medication management of the target population: general practitioners, community pharmacists, and private practice nurses * Patients who met the study's eligibility criteria regarding age and polypharmacy so that the co-designed intervention takes into account their needs and expectations, as well as their opinions regarding the methodology used (participative research). Partner patients will also be solicited.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Healthcare Professionals: In hospitals: * Geriatricians, hospital pharmacists, or registered nurses; * Practicing in a geriatric day hospital at the university hospitals in Lyon, Grenoble, Marseille, Nîmes, or Nantes; * Agree to participate in focus group meetings or the working group. In primary care facilities: * General practitioners, community pharmacists, or independent registered nurses; * Practicing within a primary care facility in the geographic areas served by the university hospitals of Lyon, Grenoble, Marseille, Nîmes, or Nantes; * Agree to participate in focus group meetings or the working group. Patients: Patients of the primary care facilities : * Patients aged 65 to 80; * Patients receiving outpatient care (not hospitalized) at a primary care facility within the geographic areas of the University Hospitals of Lyon; * Patients taking at least 5 chronic medications prescribed per day (polypharmacy); * Agree to participate in focus group meetings or the working group; Partner patients: * Partner patients of the Lyon University Hospital or the RESHAPE laboratory; * Agree to participate in meetings of the working group or the study's scientific advisory board. Exclusion Criteria: * None
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Genom att skicka in godkänner du våra Användarvillkor
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Hôpital des Charpennes, Institut du Vieillissement
Villeurbanne, 69100, France
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